ClinVar Miner

Submissions for variant NG_009814.1:g.(?_4989)_(10173_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000011713 SCV000031945 pathogenic Congenital adrenal hypoplasia, X-linked 1997-11-01 no assertion criteria provided literature only

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